IRS2
胰岛素受体
内分泌学
内科学
胰岛素
生物
葡萄糖稳态
碳水化合物代谢
超氧化物歧化酶
胰岛素受体底物
信号转导
氧化应激
细胞生物学
医学
胰岛素抵抗
作者
Akiko Taguchi,Lynn M. Wartschow,Morris F. White
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2007-07-19
卷期号:317 (5836): 369-372
被引量:521
标识
DOI:10.1126/science.1142179
摘要
Reduced insulin-like signaling extends the life span of Caenorhabditis elegans and Drosophila. Here, we show that, in mice, less insulin receptor substrate-2 (Irs2) signaling throughout the body or just in the brain extended life span up to 18%. At 22 months of age, brain-specific Irs2 knockout mice were overweight, hyperinsulinemic, and glucose intolerant; however, compared with control mice, they were more active and displayed greater glucose oxidation, and during meals they displayed stable superoxide dismutase-2 concentrations in the hypothalamus. Thus, less Irs2 signaling in aging brains can promote healthy metabolism, attenuate meal-induced oxidative stress, and extend the life span of overweight and insulin-resistant mice.
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